Have questions? Visit https://www.reddit.com/r/SNPedia

rs727504356

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504356(C;C)
Make rs727504356(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424846
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504356
ebirs727504356
HLIrs727504356
Exacrs727504356
Varsomers727504356
Maprs727504356
PheGenIrs727504356
hapmaprs727504356
1000 genomesrs727504356
hgdprs727504356
ensemblrs727504356
gopubmedrs727504356
geneviewrs727504356
scholarrs727504356
googlers727504356
pharmgkbrs727504356
gwascentralrs727504356
openSNPrs727504356
23andMers727504356
23andMe allrs727504356
SNP Nexus

SNPshotrs727504356
SNPdbers727504356
MSV3drs727504356
GWAS Ctlgrs727504356
Max Magnitude0
ClinVar
Risk rs727504356(C;C)
Alt rs727504356(C;C)
Reference rs727504356(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23894055C>G
CLNSRC
CLNACC RCV000154484.2,